Alveolar soft part sarcoma occurring in the penis of a 3-year-old boy: A rare case report.
Alveolar soft part sarcoma occurring in the penis of a 3-year-old boy: A rare case report.
复制标题
3 岁男孩阴茎发生腺泡软组织肉瘤：罕见病例报告。
DOI：
10.1097/md.0000000000008383
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发表时间：
2017-11
期刊：
影响因子：
1.6
通讯作者：
Xie M
中科院分区：
文献类型：
--
作者：
Qiu L;Li Y;Ali SI;Xie M
腺泡状软组织肉瘤是一种罕见的恶性肿瘤，好发于上肢和下肢。本文介绍了一个不寻常的情况下，ASPS涉及阴茎的一个3岁的男孩。据我们所知，这是第一例ASPS发生在儿童阴茎中。患者主诉阴茎轻微疼痛1年，阴茎内可触及软组织肿块。对阴茎进行成像。通过活检评估肿块的病理学特征。结果发现肿块是一个腺泡状软组织肉瘤，然后通过免疫组化证实。病人只接受了部分阴茎切除术，因为他的父母希望保留阴茎。术后常规化疗6个月。随访28个月，肿块无明显增大，无转移征象，ASPS可能起源于阴茎。
Alveolar soft part sarcoma (ASPS) is a rare, malignant neoplasm, which mostly occurs in the upper and lower extremities. This article presents an unusual case of ASPS involving the penis of a 3-year-old boy. To our knowledge, this is the first case of ASPS in the penis of a child. The patient complained of slight penile pain for 1 year and a soft tissue mass could be palpated in his penis. Imaging was performed on the penis. The pathological feature of the mass was evaluated through biopsy examination. It was found that the mass was an alveolar soft tissue sarcoma, which was then confirmed by immunohistochemistry. The patient only underwent a partial penectomy because his parents wished to keep the penis. Conventional chemotherapy has been performed for 6 months after the surgery. At 28-month follow-up the mass did not increase apparently, and no signs of metastasis were found. ASPS may occur originally in the penis.